5-Chloro-3-iodo-1H-indazole is a heterocyclic organic compound characterized by its indazole core, which consists of a fused benzene and pyrazole ring. The presence of chlorine and iodine substituents at the 5 and 3 positions, respectively, contributes to its unique chemical properties and reactivity. This compound typically exhibits moderate solubility in organic solvents, and its molecular structure allows for potential interactions in biological systems, making it of interest in medicinal chemistry. The halogen substituents can influence the compound's electronic properties, potentially affecting its reactivity and interactions with biological targets. Additionally, 5-Chloro-3-iodo-1H-indazole may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, due to the presence of the halogens. Its specific applications may vary, but it is often explored in the context of drug development and synthesis of more complex molecules. As with many halogenated compounds, safety precautions should be taken when handling this substance due to potential toxicity and environmental impact.

5-Chloro-3-iodo-1H-indazole

351456-45-6: 5-Chloro-3-iodo-1H-indazole is a heterocyclic organic compound characterized by its indazole core, which consists of a fused benzene and pyrazole ring. The presence of chlorine and iodine substituents at the 5 and 3 positions, respectively, contributes to its unique chemical properties and reactivity. This compound typically exhibits moderate solubility in organic solvents, and its molecular structure allows for potential interactions in biological systems, making it of interest in medicinal chemistry. The halogen substituents can influence the compound's electronic properties, potentially affecting its reactivity and interactions with biological targets. Additionally, 5-Chloro-3-iodo-1H-indazole may participate in various chemical reactions, such as nucleophilic substitutions or coupling reactions, due to the presence of the halogens. Its specific applications may vary, but it is often explored in the context of drug development and synthesis of more complex molecules. As with many halogenated compounds, safety precautions should be taken when handling this substance due to potential toxicity and environmental impact.

CAS 351456-45-6

5-Chloro-3-iodo-1H-indazole

5-Chloro-3-iodo-1H-indazole

Ref: IN-DA00BXZU

5-Chloro-3-iodo-1H-indazole

Ref: 54-OR60117

5-Chloro-3-iodo-1H-indazole

Ref: 10-F036356